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Merck
CN

F9424

Sigma-Aldrich

Fibroblast Growth Factor Receptor-2α (IIIb)/Fc Chimera human

>90% (SDS-PAGE), recombinant, expressed in baculovirus infected Sf21 cells, lyophilized powder

别名:

FGFR-2α (IIIb)/Fc

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MDL编号:
UNSPSC代码:
51111800
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生物来源

human

重组

expressed in baculovirus infected Sf21 cells

方案

>90% (SDS-PAGE)

表单

lyophilized powder

效能

1-3 ng/mL ED50

分子量

monomer calculated mol wt 66 kDa
~100 kDa by SDS-PAGE (reducing)

储存条件

avoid repeated freeze/thaw cycles (Do not store in a frost-free freezer.)

杂质

<1 EU/μg Endotoxin level (LAL test)

UniProt登记号

储存温度

−20°C

基因信息

human ... FGFR2(2263)

一般描述

FGFR2 (fibroblast growth factor receptor 2) is a member of the tyrosine kinase receptor family called FGFR. This gene is localized to human chromosome 10q26, and is composed of 2 exons.
Its ligand-binding domain in present in its extracellular region, which is composed of three immunoglobulin (Ig)-like domains. It spans the membrane once, and its tyrosine kinase domain is localized to its intracellular region. Alternative splicing of this gene gives rise to two isoforms- epithelial (FGFR2IIIb) and mesenchymal (FGFR2IIIc).

生化/生理作用

FGFR2 (fibroblast growth factor receptor 2) facilitates tumor growth, invasiveness, metastasis and angiogenesis. It plays an essential role in the development of mammary glands, and its expression is elevated in breast cancers. Studies in North Indian population suggest that polymorphisms in this gene might be linked to susceptibility to breast cancer. It is anti-apoptotic in nature, and suppresses p53-mediated apoptosis, by inducing the elevation of MDM2 levels. Mutations in this gene are linked to mild Crouzon syndrome and craniosynostosis.

外形

Lyophilized from a 0.2 μm filtered solution in phosphate buffered saline

分析说明

The bioactivity is measured by its ability to inhibit human fibroblast growth factor acidic-dependent proliferation of NR6 cells.

其他说明

Human recombinant FGFR-2α (IIIb)/Fc is a disulfide-linked homodimeric protein. As a result of glycosylation, it migrates as an approximately 100 kDa protein.

法规信息

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Aimee L Fenwick et al.
BMC medical genetics, 15, 95-95 (2014-09-02)
Mutations of fibroblast growth factor receptor 2 (FGFR2) account for a higher proportion of genetic cases of craniosynostosis than any other gene, and are associated with a wide spectrum of severity of clinical problems. Many of these mutations are highly
Zahra Saadatian et al.
Asian Pacific journal of cancer prevention : APJCP, 15(18), 7955-7958 (2014-10-09)
Breast cancer is the most common cancer among women in the world. In Iran, the incidence of breast cancer is on the increase. We here studied the association of rs1219648 in FGFR2 and rs1042522 in TP53 and their interaction in
Sarah Siddiqui et al.
PloS one, 9(10), e110426-e110426 (2014-10-22)
Genome-Wide Association Studies (GWAS) have identified Fibroblast growth factor receptor 2 (FGFR2) as a candidate gene for breast cancer with single nucleotide polymorphisms (SNPs) located in intron 2 region as the susceptibility loci strongly associated with the risk. However, replicate

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